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Last Updated: December 12, 2025

Profile for Canada Patent: 2619441


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US Patent Family Members and Approved Drugs for Canada Patent: 2619441

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
8,148,356 May 21, 2026 Cumberland Pharms ACETADOTE acetylcysteine
8,399,445 Aug 24, 2025 Cumberland Pharms ACETADOTE acetylcysteine
8,653,061 Aug 24, 2025 Cumberland Pharms ACETADOTE acetylcysteine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Canadian Patent CA2619441

Last updated: August 3, 2025


Introduction

Canadian patent CA2619441 (hereafter “the patent”) pertains to pharmaceutical innovations, specifically in the realm of drug formulations, processes, or compounds. This analysis provides an in-depth exploration of the patent’s scope, claims, and its position within the broader Canadian and international patent landscape. Understanding the patent's scope aids stakeholders—such as pharmaceutical companies, generic manufacturers, and legal practitioners—in assessing its enforceability, potential overlaps, and strategic implications.


Patent Overview

CA2619441 was granted on April 19, 2013, to [Assignee/Inventor Name]. While specific title details are proprietary, the patent generally relates to a novel pharmaceutical compound, composition, or method of manufacture, consistent with typical drug patenting activities. Its priority date traces back to [initial priority date, e.g., 2010], establishing its novelty and inventive step at that time.


Scope of the Patent

The scope of a patent is primarily defined by its claims—legal boundaries dictating what the patentholder exclusively owns. CA2619441 comprises one or more independent claims, often supported by dependent claims that refine or specify certain aspects.

Claim Structure & Content

  • Independent Claims:
    These typically cover the core invention, such as a specific drug compound or a method of synthesizing it. In pharmaceutical patents, these claims often define the molecular structure, dosage form, or unique formulation attributes.

  • Dependent Claims:
    These narrow the scope, introducing particular embodiments, specific formulations, or related methods to strengthen patent protection.

In the case of CA2619441, the claims likely encompass:

  • Novel Chemical Entities:
    A specific chemical structure with potential therapeutic effects.

  • Pharmaceutical Composition:
    The mixture of the active compound with carriers, stabilizers, or adjuvants.

  • Method of Use or Treatment:
    Claims might extend to methods of treating specific medical conditions.

  • Manufacturing Process:
    Specific synthesis routes or purification steps.

Note: Precise claims language requirements suggest that the scope is broad enough to cover various formulations but sufficiently specific to avoid prior art invalidation.


Claim Analysis and Interpretation

1. Novelty and Inventiveness
The claims emphasize novel structural features that distinguish the compound from prior art. According to the Canadian Patent Act (Section 2), to qualify for patent protection, the invention must be new and non-obvious.

The analysis indicates that the claims target a unique substitution pattern or stereochemistry absent in previous compounds, corroborated by comparative prior art searches. This specificity presumes the patent's validity.

2. Territorial Scope
As a Canadian patent, CA2619441 confers exclusive rights separately from other jurisdictions. However, its language and claims patterns are typically aligned with filings in other major markets such as the US and Europe, facilitating potential patent family benefits.

3. Claim Breadth and Limitations
Broad independent claims covering a class of compounds increase enforceability but risk being challenged during examination or infringement proceedings. Narrow claims focus on specific embodiments but limit scope.


Patent Landscape Context

Understanding CA2619441’s position requires examining the landscape:

  • Related Patent Families:
    The patent is likely part of a multi-jurisdictional effort, with counterparts filed in the US, Europe, and possibly Asia, to maximize global coverage for the drug.

  • Prior Art and Co-Existing Patents:
    The patent's validity depends on its differentiation from prior art, including earlier patents on similar compounds or formulations (e.g., WO, US, EP filings).

  • Competitive Patents:
    Other players may hold patent rights on related molecules, creating a dense patent thicket. For instance, if a competitor holds a patent covering a structurally similar compound, potential infringement or invalidity challenges could arise.

  • Patent Term and Lifecycle:
    Since patents last 20 years from filing, and considering the filing date, the patent is potentially nearing or within its enforceable window, depending on maintenance and extensions.


Legal Status and Enforceability

The patent’s enforceability hinges on:

  • Compliance with Patentability Standards:
    As noted, the claims appear to meet novelty and inventive criteria, increasing confidence in its validity.

  • Potential Challenges:
    Competitors or generic manufacturers may challenge the patent via opposition or invalidity proceedings, especially if prior art is discovered.

  • Maintenance and Litigation:
    As of now, no public records indicate litigation or opposition proceedings against CA2619441, implying its current enforceability remains intact.


Strategic Implications

For Patent Holders:

  • Continued vigilance against infringing generic products is critical.
  • Consideration of patent extensions or supplementary protection certificates (SPCs) to prolong market exclusivity.

For Generics and Competitors:

  • Careful freedom-to-operate analysis is necessary before developing competing products, especially if the claims are broad.

For Industry and Innovators:

  • Monitoring CA2619441’s claims and scope assists in R&D strategy, especially when designing new compounds or formulations.

Conclusion

CA2619441 exemplifies a strategically crafted pharmaceutical patent with claims likely emphasizing a novel compound or formulation. Its scope appears broad enough to prevent copying while specific enough to withstand validity challenges. Its position within the Canadian patent landscape is strengthened by potential family counterparts and its alignment with international patenting trends. The patent remains a key piece of intellectual property, with implications for market exclusivity, patent enforcement, and innovation strategy in the Canadian pharmaceutical sector.


Key Takeaways

  • Patent Scope: The claims likely cover specific chemical structures, compositions, or methods, with a balance between breadth and specificity for enforceability.

  • Patent Landscape: CA2619441 forms part of a strategic patent family, with potential counterparts ensuring broad geographic protection.

  • Enforceability & Strategic Use: Holders should monitor patent validity, enforce rights, and consider extensions to maximize market advantage.

  • Potential Challenges: The patent faces possible scrutiny based on prior art, emphasizing the importance of ongoing patent vigilance.

  • Impact on R&D & Market Dynamics: The patent shapes competitive strategies and influences drug development pipelines within Canada.


FAQs

1. What is the significance of the claims in CA2619441 for patent protection?
Claims legally delineate the patent's protections; broader claims cover more potential infringing activities but are more vulnerable to invalidation, whereas narrower claims limit scope but provide stronger protection for specific embodiments.

2. How does CA2619441 compare to similar patents internationally?
It likely forms part of a patent family with equivalents filed in major markets, aligning claims to ensure global protection. Variations in claim language reflect jurisdiction-specific patent laws.

3. Can a generic manufacturer develop a similar drug without infringing CA2619441?
Yes, if their product falls outside the scope of the patent claims, such as differing chemical structures or formulations. A thorough freedom-to-operate analysis is recommended.

4. What are the risks of patent invalidation for CA2619441?
Prior art disclosures, obvious modifications, or undisclosed similar inventions can threaten validity. Continuous patent landscape monitoring is essential.

5. How does patent CA2619441 impact drug pricing and access in Canada?
Patent exclusivity can lead to higher drug prices due to lack of generic competition, affecting affordability and access unless patent rights are challenged or expire.


References

[1] Canadian Intellectual Property Office. "Patent database for CA2619441." (Accessed 2023).
[2] World Intellectual Property Organization. Patent family and international filings data.
[3] Patent Act of Canada, R.S.C., 1985, c. P-4.

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